A novel frameshift CUX2 variant in a patient with epilepsy and global developmental delay: Phenotypic and genotypic expansion

European Journal of Medical Genetics · Published 2025-12-02 · DOI 10.1016/j.ejmg.2025.105064

Free full text

Authors being retrieved — see the publisher record. https://doi.org/10.1016/j.ejmg.2025.105064

Abstract

PubPorta does not have an abstract for this article yet.

Read the article at the publisher →

Publication details

Year
2025

Related articles